含4-噻唑烷酮基5-芳基苯并咪唑衍生物的设计、合成及抗菌性能评价

IF 0.4 4区 化学 Q4 CHEMISTRY, ORGANIC
N. Desai, K. Shah, P. Dave
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引用次数: 1

摘要

为了设计一类有效的抗菌药物,我们在多步常规合成下,使用不同的催化剂合成了基于4-噻唑烷酮的苯并咪唑衍生物,该衍生物具有5-亚芳基5a-o。基于光谱数据已经建立了合成化合物的结构,并且已经对化合物的抗菌活性进行了筛选。化合物5j对所有革兰氏阳性菌显示出最大效力,最小抑制浓度(MIC)在25-50μg/mL范围内,而对革兰氏阴性菌菌株观察到中等活性,MIC值为62.50μg/mL。发现化合物5n对真菌菌株最具活性,MIC值为250μg/mL。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Design, synthesis and antimicrobial evaluation of benzimidazole containing 4-thiazolidinone based 5-arylidene derivatives
In an attempt to design a potent class of antimicrobials, we have synthesized benzimidazole derivatives based on 4-thiazolidinone which possessed 5-arylidenes 5a-o by using different catalysts under multistep conventional synthesis. Structures of the synthesized compounds have been established based on spectral data and compounds have been screened for their antimicrobial activity. Compound 5j shows maximum potency against all Gram-positive bacteria with a minimum inhibitory concentration (MIC) in the range of 25-50 μg/mL while moderate activity against Gram-negative bacterial strains is observed with a MIC value of 62.50 μg/mL. Compound 5n is found to be the most active against fungal strains with a MIC value of 250 μg/mL.
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